US20130177668A1 - Solidified sugar alcohol mixture - Google Patents
Solidified sugar alcohol mixture Download PDFInfo
- Publication number
- US20130177668A1 US20130177668A1 US13/820,942 US201113820942A US2013177668A1 US 20130177668 A1 US20130177668 A1 US 20130177668A1 US 201113820942 A US201113820942 A US 201113820942A US 2013177668 A1 US2013177668 A1 US 2013177668A1
- Authority
- US
- United States
- Prior art keywords
- mixture
- solidified
- sugar alcohol
- maltitol
- mannitol
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Abandoned
Links
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- 150000005846 sugar alcohols Chemical class 0.000 title claims abstract description 122
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- MVPICKVDHDWCJQ-UHFFFAOYSA-N ethyl 3-pyrrolidin-1-ylpropanoate Chemical compound CCOC(=O)CCN1CCCC1 MVPICKVDHDWCJQ-UHFFFAOYSA-N 0.000 description 1
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- FBPFZTCFMRRESA-GUCUJZIJSA-N galactitol Chemical compound OC[C@H](O)[C@@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-GUCUJZIJSA-N 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- LPLVUJXQOOQHMX-UHFFFAOYSA-N glycyrrhetinic acid glycoside Natural products C1CC(C2C(C3(CCC4(C)CCC(C)(CC4C3=CC2=O)C(O)=O)C)(C)CC2)(C)C2C(C)(C)C1OC1OC(C(O)=O)C(O)C(O)C1OC1OC(C(O)=O)C(O)C(O)C1O LPLVUJXQOOQHMX-UHFFFAOYSA-N 0.000 description 1
- 229960004949 glycyrrhizic acid Drugs 0.000 description 1
- UYRUBYNTXSDKQT-UHFFFAOYSA-N glycyrrhizic acid Natural products CC1(C)C(CCC2(C)C1CCC3(C)C2C(=O)C=C4C5CC(C)(CCC5(C)CCC34C)C(=O)O)OC6OC(C(O)C(O)C6OC7OC(O)C(O)C(O)C7C(=O)O)C(=O)O UYRUBYNTXSDKQT-UHFFFAOYSA-N 0.000 description 1
- 235000019410 glycyrrhizin Nutrition 0.000 description 1
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- JYJIGFIDKWBXDU-MNNPPOADSA-N inulin Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)OC[C@]1(OC[C@]2(OC[C@]3(OC[C@]4(OC[C@]5(OC[C@]6(OC[C@]7(OC[C@]8(OC[C@]9(OC[C@]%10(OC[C@]%11(OC[C@]%12(OC[C@]%13(OC[C@]%14(OC[C@]%15(OC[C@]%16(OC[C@]%17(OC[C@]%18(OC[C@]%19(OC[C@]%20(OC[C@]%21(OC[C@]%22(OC[C@]%23(OC[C@]%24(OC[C@]%25(OC[C@]%26(OC[C@]%27(OC[C@]%28(OC[C@]%29(OC[C@]%30(OC[C@]%31(OC[C@]%32(OC[C@]%33(OC[C@]%34(OC[C@]%35(OC[C@]%36(O[C@@H]%37[C@@H]([C@@H](O)[C@H](O)[C@@H](CO)O%37)O)[C@H]([C@H](O)[C@@H](CO)O%36)O)[C@H]([C@H](O)[C@@H](CO)O%35)O)[C@H]([C@H](O)[C@@H](CO)O%34)O)[C@H]([C@H](O)[C@@H](CO)O%33)O)[C@H]([C@H](O)[C@@H](CO)O%32)O)[C@H]([C@H](O)[C@@H](CO)O%31)O)[C@H]([C@H](O)[C@@H](CO)O%30)O)[C@H]([C@H](O)[C@@H](CO)O%29)O)[C@H]([C@H](O)[C@@H](CO)O%28)O)[C@H]([C@H](O)[C@@H](CO)O%27)O)[C@H]([C@H](O)[C@@H](CO)O%26)O)[C@H]([C@H](O)[C@@H](CO)O%25)O)[C@H]([C@H](O)[C@@H](CO)O%24)O)[C@H]([C@H](O)[C@@H](CO)O%23)O)[C@H]([C@H](O)[C@@H](CO)O%22)O)[C@H]([C@H](O)[C@@H](CO)O%21)O)[C@H]([C@H](O)[C@@H](CO)O%20)O)[C@H]([C@H](O)[C@@H](CO)O%19)O)[C@H]([C@H](O)[C@@H](CO)O%18)O)[C@H]([C@H](O)[C@@H](CO)O%17)O)[C@H]([C@H](O)[C@@H](CO)O%16)O)[C@H]([C@H](O)[C@@H](CO)O%15)O)[C@H]([C@H](O)[C@@H](CO)O%14)O)[C@H]([C@H](O)[C@@H](CO)O%13)O)[C@H]([C@H](O)[C@@H](CO)O%12)O)[C@H]([C@H](O)[C@@H](CO)O%11)O)[C@H]([C@H](O)[C@@H](CO)O%10)O)[C@H]([C@H](O)[C@@H](CO)O9)O)[C@H]([C@H](O)[C@@H](CO)O8)O)[C@H]([C@H](O)[C@@H](CO)O7)O)[C@H]([C@H](O)[C@@H](CO)O6)O)[C@H]([C@H](O)[C@@H](CO)O5)O)[C@H]([C@H](O)[C@@H](CO)O4)O)[C@H]([C@H](O)[C@@H](CO)O3)O)[C@H]([C@H](O)[C@@H](CO)O2)O)[C@@H](O)[C@H](O)[C@@H](CO)O1 JYJIGFIDKWBXDU-MNNPPOADSA-N 0.000 description 1
- 229940029339 inulin Drugs 0.000 description 1
- BJHIKXHVCXFQLS-PQLUHFTBSA-N keto-D-tagatose Chemical compound OC[C@@H](O)[C@H](O)[C@H](O)C(=O)CO BJHIKXHVCXFQLS-PQLUHFTBSA-N 0.000 description 1
- 239000000832 lactitol Substances 0.000 description 1
- 235000010448 lactitol Nutrition 0.000 description 1
- VQHSOMBJVWLPSR-JVCRWLNRSA-N lactitol Chemical compound OC[C@H](O)[C@@H](O)[C@@H]([C@H](O)CO)O[C@@H]1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O VQHSOMBJVWLPSR-JVCRWLNRSA-N 0.000 description 1
- 229960003451 lactitol Drugs 0.000 description 1
- 239000000787 lecithin Substances 0.000 description 1
- 235000010445 lecithin Nutrition 0.000 description 1
- 229940067606 lecithin Drugs 0.000 description 1
- 239000004571 lime Substances 0.000 description 1
- 239000001115 mace Substances 0.000 description 1
- ZLNQQNXFFQJAID-UHFFFAOYSA-L magnesium carbonate Chemical compound [Mg+2].[O-]C([O-])=O ZLNQQNXFFQJAID-UHFFFAOYSA-L 0.000 description 1
- 239000001095 magnesium carbonate Substances 0.000 description 1
- 229910000021 magnesium carbonate Inorganic materials 0.000 description 1
- 235000014380 magnesium carbonate Nutrition 0.000 description 1
- HCWCAKKEBCNQJP-UHFFFAOYSA-N magnesium orthosilicate Chemical compound [Mg+2].[Mg+2].[O-][Si]([O-])([O-])[O-] HCWCAKKEBCNQJP-UHFFFAOYSA-N 0.000 description 1
- 239000000391 magnesium silicate Substances 0.000 description 1
- 235000019792 magnesium silicate Nutrition 0.000 description 1
- 229910052919 magnesium silicate Inorganic materials 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 239000001525 mentha piperita l. herb oil Substances 0.000 description 1
- 239000001683 mentha spicata herb oil Substances 0.000 description 1
- OSWPMRLSEDHDFF-UHFFFAOYSA-N methyl salicylate Chemical compound COC(=O)C1=CC=CC=C1O OSWPMRLSEDHDFF-UHFFFAOYSA-N 0.000 description 1
- 230000007483 microbial process Effects 0.000 description 1
- 244000005700 microbiome Species 0.000 description 1
- 235000019426 modified starch Nutrition 0.000 description 1
- 229930189775 mogroside Natural products 0.000 description 1
- 150000002772 monosaccharides Chemical class 0.000 description 1
- 229920003052 natural elastomer Polymers 0.000 description 1
- 229920001206 natural gum Polymers 0.000 description 1
- 229920001194 natural rubber Polymers 0.000 description 1
- ITVGXXMINPYUHD-CUVHLRMHSA-N neohesperidin dihydrochalcone Chemical compound C1=C(O)C(OC)=CC=C1CCC(=O)C(C(=C1)O)=C(O)C=C1O[C@H]1[C@H](O[C@H]2[C@@H]([C@H](O)[C@@H](O)[C@H](C)O2)O)[C@@H](O)[C@H](O)[C@@H](CO)O1 ITVGXXMINPYUHD-CUVHLRMHSA-N 0.000 description 1
- 229940089953 neohesperidin dihydrochalcone Drugs 0.000 description 1
- 235000010434 neohesperidine DC Nutrition 0.000 description 1
- 235000019412 neotame Nutrition 0.000 description 1
- HLIAVLHNDJUHFG-HOTGVXAUSA-N neotame Chemical compound CC(C)(C)CCN[C@@H](CC(O)=O)C(=O)N[C@H](C(=O)OC)CC1=CC=CC=C1 HLIAVLHNDJUHFG-HOTGVXAUSA-N 0.000 description 1
- 108010070257 neotame Proteins 0.000 description 1
- 239000001702 nutmeg Substances 0.000 description 1
- 235000015097 nutrients Nutrition 0.000 description 1
- 230000000050 nutritive effect Effects 0.000 description 1
- 239000001814 pectin Chemical class 0.000 description 1
- 229920001277 pectin Chemical class 0.000 description 1
- 235000010987 pectin Nutrition 0.000 description 1
- 239000008188 pellet Substances 0.000 description 1
- 235000019477 peppermint oil Nutrition 0.000 description 1
- 239000002304 perfume Substances 0.000 description 1
- 239000008177 pharmaceutical agent Substances 0.000 description 1
- 239000000419 plant extract Substances 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000001267 polyvinylpyrrolidone Chemical class 0.000 description 1
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
- 229920000036 polyvinylpyrrolidone Chemical class 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- HEBKCHPVOIAQTA-ZXFHETKHSA-N ribitol Chemical compound OC[C@H](O)[C@H](O)[C@H](O)CO HEBKCHPVOIAQTA-ZXFHETKHSA-N 0.000 description 1
- 238000005096 rolling process Methods 0.000 description 1
- 235000019204 saccharin Nutrition 0.000 description 1
- CVHZOJJKTDOEJC-UHFFFAOYSA-N saccharin Chemical class C1=CC=C2C(=O)NS(=O)(=O)C2=C1 CVHZOJJKTDOEJC-UHFFFAOYSA-N 0.000 description 1
- 229940081974 saccharin Drugs 0.000 description 1
- 239000000901 saccharin and its Na,K and Ca salt Chemical class 0.000 description 1
- 235000002020 sage Nutrition 0.000 description 1
- 230000001953 sensory effect Effects 0.000 description 1
- 235000002639 sodium chloride Nutrition 0.000 description 1
- BTURAGWYSMTVOW-UHFFFAOYSA-M sodium dodecanoate Chemical compound [Na+].CCCCCCCCCCCC([O-])=O BTURAGWYSMTVOW-UHFFFAOYSA-M 0.000 description 1
- 229940082004 sodium laurate Drugs 0.000 description 1
- 235000019333 sodium laurylsulphate Nutrition 0.000 description 1
- 229940045902 sodium stearyl fumarate Drugs 0.000 description 1
- DAJSVUQLFFJUSX-UHFFFAOYSA-M sodium;dodecane-1-sulfonate Chemical compound [Na+].CCCCCCCCCCCCS([O-])(=O)=O DAJSVUQLFFJUSX-UHFFFAOYSA-M 0.000 description 1
- 235000019721 spearmint oil Nutrition 0.000 description 1
- 238000001694 spray drying Methods 0.000 description 1
- 239000008107 starch Chemical class 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 229940013618 stevioside Drugs 0.000 description 1
- OHHNJQXIOPOJSC-UHFFFAOYSA-N stevioside Natural products CC1(CCCC2(C)C3(C)CCC4(CC3(CCC12C)CC4=C)OC5OC(CO)C(O)C(O)C5OC6OC(CO)C(O)C(O)C6O)C(=O)OC7OC(CO)C(O)C(O)C7O OHHNJQXIOPOJSC-UHFFFAOYSA-N 0.000 description 1
- 235000019202 steviosides Nutrition 0.000 description 1
- 235000019408 sucralose Nutrition 0.000 description 1
- BAQAVOSOZGMPRM-QBMZZYIRSA-N sucralose Chemical compound O[C@@H]1[C@@H](O)[C@@H](Cl)[C@@H](CO)O[C@@H]1O[C@@]1(CCl)[C@@H](O)[C@H](O)[C@@H](CCl)O1 BAQAVOSOZGMPRM-QBMZZYIRSA-N 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 229920003051 synthetic elastomer Polymers 0.000 description 1
- 239000003826 tablet Substances 0.000 description 1
- 150000004044 tetrasaccharides Chemical class 0.000 description 1
- 235000010436 thaumatin Nutrition 0.000 description 1
- 239000000892 thaumatin Substances 0.000 description 1
- 239000001585 thymus vulgaris Substances 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- QORWJWZARLRLPR-UHFFFAOYSA-H tricalcium bis(phosphate) Chemical compound [Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O QORWJWZARLRLPR-UHFFFAOYSA-H 0.000 description 1
- 150000004043 trisaccharides Chemical class 0.000 description 1
- 239000011782 vitamin Substances 0.000 description 1
- 235000013343 vitamin Nutrition 0.000 description 1
- 229940088594 vitamin Drugs 0.000 description 1
- 229930003231 vitamin Natural products 0.000 description 1
- 239000000341 volatile oil Substances 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 238000005550 wet granulation Methods 0.000 description 1
- 239000009637 wintergreen oil Substances 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23G—COCOA; COCOA PRODUCTS, e.g. CHOCOLATE; SUBSTITUTES FOR COCOA OR COCOA PRODUCTS; CONFECTIONERY; CHEWING GUM; ICE-CREAM; PREPARATION THEREOF
- A23G4/00—Chewing gum
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23G—COCOA; COCOA PRODUCTS, e.g. CHOCOLATE; SUBSTITUTES FOR COCOA OR COCOA PRODUCTS; CONFECTIONERY; CHEWING GUM; ICE-CREAM; PREPARATION THEREOF
- A23G3/00—Sweetmeats; Confectionery; Marzipan; Coated or filled products
- A23G3/34—Sweetmeats, confectionery or marzipan; Processes for the preparation thereof
- A23G3/36—Sweetmeats, confectionery or marzipan; Processes for the preparation thereof characterised by the composition containing organic or inorganic compounds
- A23G3/38—Sucrose-free products
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23G—COCOA; COCOA PRODUCTS, e.g. CHOCOLATE; SUBSTITUTES FOR COCOA OR COCOA PRODUCTS; CONFECTIONERY; CHEWING GUM; ICE-CREAM; PREPARATION THEREOF
- A23G3/00—Sweetmeats; Confectionery; Marzipan; Coated or filled products
- A23G3/34—Sweetmeats, confectionery or marzipan; Processes for the preparation thereof
- A23G3/346—Finished or semi-finished products in the form of powders, paste or liquids
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23G—COCOA; COCOA PRODUCTS, e.g. CHOCOLATE; SUBSTITUTES FOR COCOA OR COCOA PRODUCTS; CONFECTIONERY; CHEWING GUM; ICE-CREAM; PREPARATION THEREOF
- A23G4/00—Chewing gum
- A23G4/06—Chewing gum characterised by the composition containing organic or inorganic compounds
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23G—COCOA; COCOA PRODUCTS, e.g. CHOCOLATE; SUBSTITUTES FOR COCOA OR COCOA PRODUCTS; CONFECTIONERY; CHEWING GUM; ICE-CREAM; PREPARATION THEREOF
- A23G4/00—Chewing gum
- A23G4/06—Chewing gum characterised by the composition containing organic or inorganic compounds
- A23G4/10—Chewing gum characterised by the composition containing organic or inorganic compounds characterised by the carbohydrates used, e.g. polysaccharides
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
- A23L27/00—Spices; Flavouring agents or condiments; Artificial sweetening agents; Table salts; Dietetic salt substitutes; Preparation or treatment thereof
- A23L27/30—Artificial sweetening agents
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
- A23L27/00—Spices; Flavouring agents or condiments; Artificial sweetening agents; Table salts; Dietetic salt substitutes; Preparation or treatment thereof
- A23L27/30—Artificial sweetening agents
- A23L27/33—Artificial sweetening agents containing sugars or derivatives
- A23L27/34—Sugar alcohols
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
- A23L29/00—Foods or foodstuffs containing additives; Preparation or treatment thereof
- A23L29/30—Foods or foodstuffs containing additives; Preparation or treatment thereof containing carbohydrate syrups; containing sugars; containing sugar alcohols, e.g. xylitol; containing starch hydrolysates, e.g. dextrin
- A23L29/37—Sugar alcohols
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23P—SHAPING OR WORKING OF FOODSTUFFS, NOT FULLY COVERED BY A SINGLE OTHER SUBCLASS
- A23P10/00—Shaping or working of foodstuffs characterised by the products
- A23P10/20—Agglomerating; Granulating; Tabletting
- A23P10/28—Tabletting; Making food bars by compression of a dry powdered mixture
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23V—INDEXING SCHEME RELATING TO FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES AND LACTIC OR PROPIONIC ACID BACTERIA USED IN FOODSTUFFS OR FOOD PREPARATION
- A23V2002/00—Food compositions, function of food ingredients or processes for food or foodstuffs
Definitions
- the present invention relates to solidified sugar alcohol mixtures containing more than 70% w/w and less than 95% w/w maltitol and a process for preparing these and the corresponding chewing gum composition and tablets containing the solidified sugar alcohol mixtures.
- Sugar alcohol and sugar alcohol mixtures are used to a great extent as additives and carriers, inter alia, for tablets for chewing and sucking, chewing gum and other products of the confectionery industry.
- Sugar alcohols are generally produced by hydrogenation of their underlying carbohydrates.
- Maltitol itself is a sugar alcohol obtained through catalytic hydrogenation of maltose. Crystalline maltitol and crystalline mixture solid containing it are widely used in food, pharmaceuticals, and cosmetics due to their low hygroscopicity and excellent performance as an excipient.
- EP 0 816 373 describes a process for manufacturing crystalline maltitol and crystalline mixture solid containing this and more particularly to a process for manufacturing in any desired ratio both crystalline maltitol and crystalline mixture solid containing this.
- U.S. Pat. No. 6,165,511 describes a polyol composition useful for the production of tablets and which is obtained by co-spray drying or co-fluidized bed granulating at least two polyols, one of which is non-hygroscopic polyol and the non-hygroscopic polyol is present in an amount of at least 80% by weight.
- U.S. Pat. No. 5,651,829 relates to a crystalline maltitol composition which essentially exhibits a porous and honeycombed structure and which possesses a very high degree of maltitol purity and a low density.
- EP 1 738 657 describes a powdery sugar alcohol composition for tabletting.
- the composition consists essentially of a crystalline sugar alcohol and an amorphous sugar alcohol provided that the composition comprises 2-12% of amorphous sorbitol.
- WO 2005037849 relates to a process for preparing solidified maltitol.
- the solidified maltitol is prepared by turbulating a maltitol powder with gas and contacting it with a maltitol containing syrup wherein the quantity of the powder is a the quantity of the syrup.
- the solidified maltitol has superior properties in bakery products. It is further suitable in other food products such as confectionery, chewing gum coatings and tablets.
- the current invention relates to a solidified sugar alcohol mixture containing maltitol characterized in that the mixture is comprising less than 95% w/w maltitol based on dry matter of mixture and upon tabletting a fraction of said mixture having an average particle size of from 150 to 250 microns, a hardness of from 70 to 220 N is obtained at a compression force of 5 kN to 25 kN and said solidified sugar alcohol mixture is containing more than 70% w/w maltitol based on dry matter of mixture and it is comprising from 2-10% w/w mannitol based on dry matter of the mixture, preferably from 3 to 6% w/w mannitol.
- the current invention further relates to a process for preparing a solidified sugar alcohol mixture previously described and said process is comprising the following steps:
- the current invention relates to chewing gum composition containing a gum base, a flavouring agent and sweetening filler comprising the previously described solidified mixture of sugar alcohols.
- the current invention relates to a tablet comprising the previously described solidified mixture of sugar alcohols.
- the current invention relates to a solidified sugar alcohol mixture containing maltitol characterized in that the mixture is comprising less than 95% w/w maltitol based on dry matter of mixture and upon tabletting a fraction of said mixture having an average particle size of from 150 to 250 microns, a hardness of from 70 to 220 N is obtained at a compression force of 5 kN to 25 kN and said solidified sugar alcohol mixture is containing more than 70% w/w maltitol based on dry matter of mixture and it is comprising from 2-10% w/w mannitol based on dry matter of the mixture, preferably from 3 to 6% w/w mannitol.
- Sugar alcohol also known as polyol, polyhydric alcohol or polyol, is a hydrogenated (reduced) form of carbohydrates wherein the carbonyl group (being aldehyde, acetal, or ketone function) has been reduced to a primary or secondary hydroxyl groups.
- Maltitol also known as 4-O- ⁇ -glucopyranosyl-D-sorbitol, is industrially obtained by hydrogenation of maltose. It is of great interest due to the fact that it is more chemically stable and is containing less calories than sucrose, while advantageously possessing organoleptic properties which are very akin to those of sucrose.
- Solidified sugar alcohol mixtures are mixtures of sugar alcohols that have turned from a liquid or melted state into a solidified state at room temperature (being around 20 to 25° C.).
- the mixture may contain crystalline material as well as amorphous material.
- the solidified mixture of sugar alcohols according to the current invention is characterized in that it is containing more than 70% w/w maltitol, preferably more than 80% w/w maltitol, more preferably more than 88% w/w maltitol.
- the content is always expressed based upon the dry matter content of the total mixture.
- the solidified mixture of sugar alcohols according to the current invention is comprising from more than 88% w/w maltitol to less than 95% w/w maltitol.
- the solidified mixture is containing more than 70% w/w, preferably more than 88% w/w maltitol and less than 94% w/w maltitol. The w/w is measured by high performance liquid chromatography.
- the solidified mixture of sugar alcohols according to the current invention is comprising from 2-10% w/w mannitol based on dry matter of the mixture, preferably from 3 to 6% w/w mannitol.
- the solidified sugar alcohol mixture containing between 70% w/w and 95% w/w maltitol, and from 2-10% w/w mannitol, preferably from 3 to 6% w/w mannitol, is further comprising from 0.1 to 5% w/w sorbitol based on dry matter of the mixture, preferably it is comprising from 0.1 to below 2% w/w sorbitol.
- the solidified mixture of sugar alcohols according to the current invention is thus comprising from more than 88% w/w maltitol to less than 95% w/w maltitol, from 2-10% w/w mannitol, preferably from 3 to 6% w/w mannitol, and is further comprising from 0.1 to 5% w/w sorbitol based on dry matter of the mixture, preferably it is comprising from 0.1 to below 2% w/w. sorbitol.
- the hardness obtained upon tabletting said mixtures indicates a measure for the reaction of the mixture of sugar alcohols towards a pressure forced onto the mixture.
- the current solidified sugar alcohol mixture containing more than 70% w/w maltitol based on dry matter of mixture and less than 95% w/w maltitol based on dry matter of mixture and comprising from 2-10% w/w mannitol based on dry matter of the mixture, preferably from 3 to 6% w/w mannitol is having upon tabletting a fraction of said mixture having an average particle size of from 150 to 250 microns, a hardness of from 70 to 220 N, obtained at a compression force of 5 kN to 25 kN, preferably at a compression force of 10 kN, 20 kN and 25 kN.
- the solidified mixture of sugar alcohols according to the current invention is further characterized in that it is having an average particle size diameter (d 50 ) of smaller than 90 microns, preferably smaller than 60 microns.
- the solidified mixture of sugar alcohols according to the current invention is having an average particle size diameter (d 50 ) of from 20 to 60 microns ( ⁇ m). Average particle size diameters (d 50 ) of 30 ⁇ m, 40 ⁇ m or 50 ⁇ m are obtainable.
- the solidified mixture of sugar alcohols according to the current invention is having an average particle size diameter (d 50 ) of from 150 to 250 microns ( ⁇ m).
- the average particle size diameter is determined by using Laser light diffraction analyser LS 13320.
- the solidified mixture of sugar alcohols according to the current invention can be further characterized by its heat of fusion, more particularly the solidified mixture of sugar alcohols according to the current invention which is having an average particle size diameter (d 50 ) smaller than 90 microns, preferably smaller than 60 ⁇ m or from 20 to 60 ⁇ m, is further characterized by its heat of fusion.
- d 50 average particle size diameter
- Heat of fusion also known as enthalpy of fusion or specific melting heat, is the amount of thermal energy which must be absorbed for 1 gram of substance to change states from solid to liquid.
- the heat of fusion is expressed in J/g and is measured with Differential Scanning Calorimetry (DSC) while using a heating rate of 4° C./min and a start temperature of 30° C. and end temperature of 170° C.
- the heat of fusion of the solidified mixture of sugar alcohols according to the current invention and further having an average particle size smaller than 90 microns is from 135 to 145 J/g. Values of 138 J/g or 143 J/g are obtainable.
- This solidified mixture of sugar alcohols is having, a major peak of melting temperature between 138-145° C. Values of 142° C., 143° C. or 145° C. are obtainable for these solidified sugar alcohol mixtures.
- the solidified sugar alcohol mixture of the current invention which is further having an average particle size smaller than 90 microns, contains on dry matter from 3 to 25% amorphous maltitol, from 5 to 20%, from 5 to 15%, or values of amorphous maltitol of 5% and 7% amorphous maltitol are obtainable.
- solidified sugar alcohol mixtures have no peak of melting for crystalline mannitol and no peak for crystalline sorbitol.
- the total amount of amorphous sugar alcohol equals 100% minus the calculated amount of crystalline maltitol, since no other crystalline sugar alcohols were determined.
- the solidified sugar alcohol mixture of the current invention having an average particle size diameter (d 50 ) smaller than 90 microns, contains from 10 to 30% amorphous sugar alcohols, preferably from 12 to 25%, from 12% to 20%, or 13% to 17% based upon dry matter.
- the solidified mixture of sugar alcohols according to the current invention and which is having an average particle size diameter (d 50 ) smaller than 90 microns is further characterized in that it is having a specific surface area greater than 0.40 m 2 /g, preferably greater than 0.45 m 2 /g, more preferably at least 0.50 m 2 /g.
- the specific surface area may be higher than 0.8 m 2 /g, from 0.8 to 1.30 m 2 /g. Values of 0.9, 1.1 and 1.27 m 2 /g are obtainable.
- the specific surface area is measured with BET method.
- the apparent density is measured by determining the weight of 250 ml of the powder in a flask of 250 ml.
- solidified sugar alcohol mixtures are particular suitable for the preparations of food, feed, pharma, personal care and cosmetic products, detergents, fertilizer or agrochemical products.
- the solidified sugar alcohol mixtures of the current invention can be used in food products, animal feed, health food, dietetic products, animal medicine, with bath agent, in agrochemical products, with fertilizer, with plant granules, with plant seeds or seed grains, and any other product being it ingested by humans and/or animals or any other product which can benefit from the improved properties of the solidified sugar alcohol mixtures of the current invention.
- the solidified sugar alcohol mixtures of the current invention can further be used as carrier for additives based on enzymes or microorganisms, detergent tablets, vitamins, flavors, perfumes, acids, sweeteners or various active ingredients with medicinal or non-medicinal applications.
- the current invention relates to a process for preparing a solidified sugar alcohol mixture according to the current invention and said process is comprising the following steps:
- the current invention describes the process for preparing a solidified sugar alcohol mixture containing maltitol characterized in that the mixture is comprising less than 95% w/w maltitol based on dry matter of mixture and upon tabletting a fraction of said mixture having an average particle size of from 150 to 250 microns, a hardness of from 70 to 220 N is obtained at a compression force of 5 kN to 25 kN and said solidified sugar alcohol mixture is containing more than 70% w/w maltitol based on dry matter of mixture and it is comprising from 2-10% w/w mannitol based on dry matter of the mixture, preferably from 3 to 6% w/w mannitol and it is comprising the following steps:
- the sugar alcohol also known as polyol, or polyhydric alcohol
- polyol is a hydrogenated (reduced) form of carbohydrates wherein the carbonyl group (being aldehyde, acetal, or ketone function) has been reduced to a primary or secondary hydroxyl groups.
- the sugar alcohol of the current invention is not necessarily obtained by reduction or hydrogenation of the carbohydrate.
- the sugar alcohol is selected from tetritols, pentitols, hexitols, hydrogenated disaccharides, hydrogenated trisaccharides, hydrogenated tetrasaccharides, hydrogenated maltodextrins and mixtures thereof.
- the polyol may be selected from the group consisting of erythritol, threitol, arabinitol, xylitol, ribitol, allitol, altritol, gulitol, galactitol, mannitol, sorbitol, talitol, maltitol, isomaltitol, isomalt, lactitol, and mixtures thereof.
- the process of the current invention is characterized in that the mixture of sugar alcohols is comprising between 70% w/w and 95% w/w maltitol. More preferably it is comprising from 2-10% w/w mannitol based on dry matter of the mixture, preferably from 3 to 6% w/w.
- a starting sugar alcohol mixture that can be used in the process of the current invention is containing between 70%w/w and 95% w/w maltitol, and from 2-10% w/w mannitol, preferably from 3 to 6% w/w mannitol, and is further comprising from 0.1 to 5% w/w sorbitol based on dry matter of the mixture, preferably it is comprising from 0.1 to below 2% w/w sorbitol.
- the mixture of sugar alcohols is thus comprising from more than 88% w/w maltitol to less than 95% w/w maltitol, from 2-10% w/w mannitol, preferably from 3 to 6% w/w mannitol, and is further comprising from 0.1 to 5% w/w sorbitol based on dry matter of the mixture, preferably it is comprising from 0.1 to below 2% w/w. sorbitol.
- the sugar alcohols can be mixed in solid state or can be mixed as liquid compositions and the mixture of sugar alcohols is brought to a residual moisture content of below 5%.
- the liquid mixture of sugar alcohols is evaporated at a temperature of from 40° C. to 135° C., preferably from 60° C. to 135° C. Typical suitable temperatures are above 120° C. and about 130° C.
- the moisture content is below 5%, preferably below 4%.
- the mixture of sugar alcohols that is having a residual moisture content of below 5% is fed through feed lines to an extruder.
- the mixture is heated to a temperature from 75° C. to 135° C.
- the mixture of sugar alcohols is fed with a feed rate of 40 to 120 kg/h, preferably from 80-95 kg/h and the sugar alcohol mixture is mixed in the extruder for about 5 to 30 minutes, preferably from 10 to 20 minutes, depending upon the feed rate.
- the retention time is a function of the feed rate, the volume of the product in the extruder at a given time and the size of the extruder.
- the sugar alcohol mixture solidifies in the extruder.
- extruder is Readco from Readco Manufacturing Inc.
- the mechanistics are for instance described in U.S. Pat. No. 3,618,902.
- Other types of extruders may be useful and it is up to the skilled person, based upon the current disclosure, to determine the type and appropriate parameters that allow preparing the solidified sugar alcohol mixture of the current invention.
- the extrudate is dropped from the extruder onto a belt and permitted to age (to cure) in the ambient temperature from 10 seconds to 15 minutes. Alternatively, the extrudate is conveyed to paddle blenders to allow time to age.
- the process is further comprising a milling step, more preferably the milling step is a jet-milling step of the aged, extruded, solidified sugar alcohol mixture.
- the solidified mixture of sugar alcohols according to the current invention and which is having an average particle size diameter (d 50 ) of from 150 to 250 microns can be obtained by common milling processes known in the art, while the solidified mixture of sugar alcohols according to the current invention and which is having an average particle size diameter (d 50 ) smaller than 90 microns is preferably obtainable through the process of the current invention including a jet-milling step of the aged, extruded, solidified sugar alcohol mixture.
- the solidified sugar alcohol mixture is ground in a jet-mill, a counterjet mill or classifier, suitable to grind the product to a product having an average particle size diameter below 90 microns. Suitable processes are described in WO 94/21827 and WO 2009/016133.
- the current invention relates to a chewing gum composition containing a gum base, and a sweetening filler comprising a solidified sugar alcohols mixture of current invention which is having an average particle size diameter (d 50 ) smaller than 90 microns.
- a sweetening filler comprising a solidified sugar alcohols mixture that is comprising between 70% w/w and 95% w/w maltitol having an average particle size diameter of smaller than 90 microns.
- the chewing gum composition comprises a solidified sugar alcohol mixture having an average particle size diameter of smaller than 90 microns and which is comprising from 2-10% w/w mannitol based on dry matter of the mixture, preferably from 3 to 6% w/w and is further comprising from 0.1 to 5% w/w sorbitol based on dry matter of the mixture and preferably it is comprising from 0.1 to below 2% w/w sorbitol.
- the solidified mixture of sugar alcohols according to the current invention is thus comprising from more than 88% w/w maltitol to less than 95% w/w maltitol, from 2-10% w/w mannitol, preferably from 3 to 6% w/w mannitol, and is further comprising from 0.1 to 5% w/w sorbitol based on dry matter of the mixture, preferably it is comprising from 0.1 to below 2% w/w sorbitol.
- the gum base portion is retained in the mouth throughout chewing while the sweetening filler in the soluble portion dissipates with a portion of the flavour over time during chewing.
- the soluble portion contains additional components such as flavouring agents, colouring agents, other sweeteners, pharmaceutical agents, nutrients and the like.
- the composition of the gum base typically determines whether the gum is considered as chewing gum, bubble gum or a functional gum.
- the gum base is inert and non-nutritive and is made from combinations of the following components: elastomers, softeners (plasticisers) emulsifiers, resins and fillers.
- Elastomers provide the rubbery, cohesive nature to the gums and can include for example, one or more natural rubbers, natural gums or synthetic elastomers. Resins can be used to vary the firmness of the gum base and aid in softening the elastomer component of the gum base.
- Softeners also known as plasticizers
- the softeners may include oils, fats, waxes and emulsifiers. Emulsifiers aid in forming uniform dispersion of the non-soluble/soluble phases and also can have plasticising properties.
- the chewing gum composition optionally may include adjuvants or fillers in either the gum base and/or soluble portion of the composition. Suitable adjuvants or fillers include, for example, lecithin, calcium carbonate, magnesium carbonate, magnesium silicate, ground limestone, aluminium hydroxide, aluminium silicate, talc, clay, alumina, titanium oxide and calcium phosphate. Colouring agents and whiteners can be optionally added to the chewing gum composition. Additional components of the gum base optionally can include one or more antioxidants, preservatives and/or intense sweeteners.
- the flavouring agents include natural and artificial flavours and combinations thereof.
- the flavouring agent can be an essential oil, such as an oil derived from a plant or a fruit, peppermint oil, spearmint oil, other mint oils, clove oil, cinnamon oil, oil of wintergreen, bay, thyme, cedar leaf, nutmeg, allspice, sage, mace, almond, anise and the like.
- the flavouring agent may be a plant extract or a fruit essence such as apple, banana, watermelon, pear, peach, grape, strawberry, raspberry, cherry, plum, pineapple, and apricot or a combination of fruit flavourings (e.g. Tutti frutti).
- flavouring agent can be a citrus flavour, such as extract, essence or oil of lemon, lime, orange, tangerine, grapefruit, or kumquat. These flavouring agents may be used in liquid or solid form and may be used individually or in admixture.
- the intense sweeteners may include, but are not limited to, sucralose, aspartame, salts of acesulfame (e.g. acesulfame-K), alitame, saccharin and its salts, cyclamic acids and its salts, glycyrrhizin, dihydrochalcones (e.g. neohesperidin dihydrochalcone) thaumatin, monellin, neotame, stevioside, mogroside, phyllodulcin, mabinlin, brazzein, pentadin, and the like, alone or in combination.
- acesulfame e.g. acesulfame-K
- alitame e.g. acesulfame-K
- saccharin and its salts cyclamic acids and its salts
- glycyrrhizin dihydrochalcones (e.g. n
- sweeteners may be present such as tagatose, other sugar alcohols, trehalose, isomaltulose and the like, alone or in combination.
- Chewing gum compositions can be prepared using known techniques.
- chewing can be manufactured by sequentially adding the various chewing gum ingredients to any commercial available mixer known in the art, see for example U.S. Pat. No. 5,334,397. After the ingredients (including the solidified sugar alcohol mixture according to the current invention) have been thoroughly mixed, the gum mass can be discharged from the mixer and shaped into the desired forms such as by rolling into sheets and cutting to sticks, extruding into chunks, or casting into pellets or tablets.
- a variety of chewing gum and bubble gum shapes are possible, including sticks, chunks, tablets, centre filled, balls, fruit shapes, cigarette shaped, coins, tube gums and compressed powder gums.
- the chewing gum prepared with the solidified sugar alcohol mixture of current invention allowed to obtain chewing gums with a hardness in the range of 2900 to 6000 g (measured after 1 month storage at 20° C. at 40% relative humidity) and the thus obtained chewing gum each have a higher hardness than the hardness of the chewing gum based upon milled crystalline maltitol or the corresponding milled physical blends.
- the granulometry was comparable with the granulometry of the products of the current invention.
- the current invention relates to a tablet comprising tablet ingredients and the solidified sugar alcohol according to the current invention and which is having an average particle size diameter (d 50 ) of from 150 to 250 microns.
- the tablet comprising a solidified mixture of sugar alcohols which is having an average particle size diameter (d 50 ) of from 150 to 250 microns and that is comprising between 70% w/w and 95% w/w maltitol having a hardness of from 70 N to 220 N at a compression force of 5 kN to 25 kN, preferably at a compression force of 10 kN, 20 kN and 25 kN.
- the tablet is comprising a solidified mixture of sugar alcohol which is having an average particle size diameter (d 50 ) of from 150 to 250 microns and which in itself is comprising from 2-10% w/w mannitol based on dry matter of the mixture, preferably from 3 to 6% w/w and is further comprising from 0.1 to 5% w/w sorbitol based on dry matter of the mixture.
- d 50 average particle size diameter
- the tablet containing the solidified sugar alcohol mixture which is having an average particle size diameter (d 50 ) of from 150 to 250 microns and is containing between 70% w/w and 95% w/w maltitol, and from 2-10% w/w mannitol, preferably from 3 to 6% w/w mannitol, and is further comprising from 0.1 to 5% w/w sorbitol based on dry matter of the mixture.
- the tablet is based upon the solidified mixture of sugar alcohols according to the current invention which is having an average particle size diameter (d 50 ) of from 150 to 250 microns and which is comprising from more than 88% w/w maltitol to less than 95% w/w maltitol, from 2-10% w/w mannitol, preferably from 3 to 6% w/w mannitol, and is further comprising from 0.1 to 5% w/w sorbitol based on dry matter of the mixture, preferably it is comprising from 0.1 to below 2% w/w. sorbitol.
- d 50 average particle size diameter
- tablette includes any tablet, in particular tablets in any form, shape and of any physical, chemical or sensory property, and tablets for any route of administration, indication and application.
- Additives or auxiliary substances such as lubricants can be added and may include sweeteners, flavorings, taste substances and coloring agents, food-compatible acids, disintegrants, monosaccharides, disaccharides, sugar alcohols, starch, starch derivatives, pectins, polyvinylpyrrolidone, cellulose, cellulose derivatives, intense sweeteners, stearic acid or the salts thereof, or inulin.
- a lubricant agent in tablet formation magnesium stearate, calcium stearate, stearic acid, sucrose fatty acid esters, and/or talc and the like can be added according to needs.
- surface active agents such as sodium lauryl sulfate, propylene glycol, sodium dodecanesulfonate, sodium oleate sulfonate, and sodium laurate mixed with stearates and talc, sodium stearyl fumarate, sucrose fatty acid esters, and the like can be added according to needs.
- the current invention relates to a process for preparing these tablets.
- Said process for preparing the tablet according to the current invention comprises the following steps:
- the process for preparing the tablets of the current invention can be very simple, by blending a lubricant with the solidified sugar alcohol mixture which is having an average particle size diameter (d 50 ) of from 150 to 250 microns followed by tabletting at compression forces from 5 to 25 kN.
- solidified sugar alcohol mixture which is having an average particle size diameter (d 50 ) smaller than 90 microns can be granulated, followed by blending with lubricant and tabletting at compressing forces from 5 to 25 kN.
- Granulation methods can be divided in two basic types, namely wet methods, which use a liquid in the process, and dry methods in which no liquid is used.
- Wet granulation is most often used and involves many steps, including: agglomerating (granulating) of dry primary powder particles of active ingredients and excipients in the presence of a granulating fluid upon agitation using low-shear or high-shear mixers or fluidized beds, wet sieving (wet screening) to remove larger lumps, drying the granulated product, and milling or sieving (screening) the dried granulated product to achieve a granulated product having the desired granule size distribution.
- the obtained granulation may subsequently be tabletted.
- Fine powdery material (product: example 1a) was obtained, having a dry substance of 99.5% and an average (median) granulometry size (d50) of 39.4 ⁇ m, (measured by Laser light diffraction analyser LS 1332).
- the other fraction >900 ⁇ m was dried and milled and a coarse fraction (product: example 1b) was obtained with an average granulometry size (d50) of 178 ⁇ m, (measured by Laser light diffraction analyser LS 1332).
- the solidified sugar alcohol contained 91.32% maltitol, 5.15% mannitol, 1.26% sorbitol and 2.27% higher polyols, according to HPLC analysis.
- the apparent (loose) density of product example 1 b is 0.670 g/ml.
- Fine powdery material (product: example 2a) was obtained having a dry substance of 99.5% and an average (median) granulometry size (d50) of 29.7 ⁇ m, (measured by Laser light diffraction analyser LS 1332).
- the solidified sugar alcohol contained 91.32% maltitol, 5.12% mannitol, 1.27% sorbitol and 2.29% higher polyols, according to HPLC analysis.
- the apparent (loose) density of product example 2b is 0.720 g/ml.
- the solidified sugar alcohol contained 93.82% maltitol, 3.52% mannitol, 0.86% sorbitol and 1.79% higher polyols, according to HPLC analysis.
- the apparent (loose) density of product example 3b is 0.680 g/ml.
- CB Ingredients (%) 1 Gum Base - Cafosa gum base 35 Sweetener - solidified sugar alcohol 53 mixture - example fraction a (fine product) Maltitol syrup 16303L (Cargill) 10.0 Glycerin 2.0 Total 100 1 CB % is commercial basis”, refers to the compounds in the recipe that are used ‘as is’ and used in the state they are commercially available. The sweetener is added at the dry substance that is obtained in the process described before.
- the chewing gum was made by preheating a Z-blade apparatus (Winkworth Model MZ 4/2) to 50° C.
- Half of the sweetener composition was added to the gum base in the Z-blade and mixed for 5 minutes at speed 4.
- the remaining sweetener was then added in the blender and mixed for further 5 minutes.
- the maltitol syrup was added and mixed again for 5 minutes.
- Glycerin was then added and mixed for 5 minutes. Liquid flavor was lastly added and the entire content in the blender was mixed not more than 3 to 5 minutes.
- the chewing gum has been tested for their hardness while stored in a cabinet (25° C.-40% Relative Humidity).
- the gum is completely sealed in plastic), and compared with chewing gum prepared from crystalline maltitol or a regular physical blend of maltitol and mannitol.
- Hardness measurements (g). Storage conditions: Room Temperature (20° C.) 1 day - A week - Cabinet Cabinet A month - Storage Storage cabinet Samples - chewing gum Average Average Storage containing materials from Hard. Hard. Average Hard.
- Example 1a (fine 3802 4481 3669 product)
- Example 2a (fine 5705 6660 5915 product)
- Example 3a (fine 3462 4009 2985 product) Milled Crystalline 1794 3048 2586 Maltitol (CH 16385 - Cargill Milled Physical 1830 2884 2466 Blend maltitol mannitol as in example 1 or 2 Milled Physical 1772 2883 2135 Blend maltitol and mannitol as in example 3
- the chewing gum prepared with the fine products of solidified sugar alcohol mixture of example 1 a to 3a allowed to obtain chewing gums with a hardness in a range of 2900 to 6000 g (measured after 1 month storage at 20° C. at 40% relative humidity) and the thus obtained chewing gum each had a higher hardness than the hardness of the chewing gum based upon milled crystalline maltitol or the corresponding milled blends.
- Tablets could be prepared with the solidified mixtures of the current invention.
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Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
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EP10009270.9 | 2010-09-07 | ||
EP10009270 | 2010-09-07 | ||
PCT/EP2011/004421 WO2012031720A1 (en) | 2010-09-07 | 2011-09-01 | Solidified sugar alcohol mixture |
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US20130177668A1 true US20130177668A1 (en) | 2013-07-11 |
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US13/820,942 Abandoned US20130177668A1 (en) | 2010-09-07 | 2011-09-01 | Solidified sugar alcohol mixture |
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US (1) | US20130177668A1 (zh) |
EP (1) | EP2613645A1 (zh) |
JP (1) | JP2013536694A (zh) |
KR (1) | KR20130138774A (zh) |
CN (1) | CN103200828A (zh) |
BR (1) | BR112013005440A2 (zh) |
MX (1) | MX2013002326A (zh) |
RU (1) | RU2013115388A (zh) |
WO (1) | WO2012031720A1 (zh) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
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WO2016001586A1 (fr) * | 2014-07-01 | 2016-01-07 | Roquette Freres | Nouvelle composition de produit de confiserie |
US20160209124A1 (en) * | 2013-08-29 | 2016-07-21 | Board Of Regents, The University Of Texas System | Thermal storage units, components thereof, and methods of making and using them |
CN108697114A (zh) * | 2016-02-17 | 2018-10-23 | 罗盖特公司 | 增强的风味释放口香糖组合物 |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20150201644A1 (en) * | 2012-08-22 | 2015-07-23 | Intercontinental Great Brands Llc | Chewing gum compositions and methods of making thereof |
FR3009926B1 (fr) * | 2013-09-02 | 2017-08-11 | Roquette Freres | Utilisation d'un agent anti mottant pour ameliorer la durete de chewing-gum contenant du maltitol sous forme pulverulente |
JP6489871B2 (ja) * | 2014-02-28 | 2019-03-27 | クラシエフーズ株式会社 | チューインガム |
AU2015265470A1 (en) * | 2014-05-29 | 2016-11-24 | Novartis Ag | Ceritinib formulation |
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US4831129A (en) * | 1985-10-02 | 1989-05-16 | Roquette Freres | Directly compressible powdered maltitol and its process of preparation |
US5651829A (en) * | 1995-03-29 | 1997-07-29 | Roquette Freres | Maltitol composition and process for preparing it |
US20030099701A1 (en) * | 2001-05-10 | 2003-05-29 | Yamanouchi Pharmaceutical Co., Ltd. | Quick-disintegrating tablet in buccal cavity and manufacturing method thereof |
US20080020008A1 (en) * | 2005-01-24 | 2008-01-24 | Nikken Fine Chemical Co., Ltd. | Eutectic Crystalline Sugar Alcohol and Manufacturing Method Thereof |
US20110097401A1 (en) * | 2009-06-12 | 2011-04-28 | Meritage Pharma, Inc. | Methods for treating gastrointestinal disorders |
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US3618902A (en) | 1969-11-14 | 1971-11-09 | Teledyne Inc | Continuous mixer |
US5334397A (en) | 1992-07-14 | 1994-08-02 | Amurol Products Company | Bubble gum formulation |
FI96041C (fi) | 1993-03-19 | 1996-04-25 | Sucros Oy | Makeutusaine, menetelmä sen valmistamiseksi ja sen käyttö |
FR2715538B1 (fr) * | 1994-02-01 | 1996-04-26 | Roquette Freres | Composition de chewing-gum présentant une qualité organoleptique améliorée et procédé permettant de préparer un tel chewing-gum. |
IL117623A (en) * | 1995-03-29 | 2000-01-31 | Roquette Freres | Maltitol composition and its preparation |
DE19615418A1 (de) | 1996-04-22 | 1997-10-23 | Merck Patent Gmbh | Polyol-Zusammensetzung |
JP4711471B2 (ja) | 1996-07-05 | 2011-06-29 | 三菱商事フードテック株式会社 | 結晶マルチトール及びそれを含有する含蜜結晶の製造方法 |
KR20060089224A (ko) | 2003-10-21 | 2006-08-08 | 카아길, 인코포레이팃드 | 응고된 말티톨의 제조방법 및 식품과 의약품에서의 이의용도 |
JP5110810B2 (ja) * | 2005-06-28 | 2012-12-26 | 上野製薬株式会社 | 打錠用糖アルコール粉末組成物 |
KR20070001013A (ko) | 2005-06-28 | 2007-01-03 | 가부시키가이샤 우에노 세이야꾸 오요 겡뀨조 | 정제화용 당알코올 조성물 |
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2011
- 2011-09-01 US US13/820,942 patent/US20130177668A1/en not_active Abandoned
- 2011-09-01 BR BR112013005440A patent/BR112013005440A2/pt not_active IP Right Cessation
- 2011-09-01 KR KR1020137008834A patent/KR20130138774A/ko not_active Application Discontinuation
- 2011-09-01 JP JP2013527487A patent/JP2013536694A/ja active Pending
- 2011-09-01 MX MX2013002326A patent/MX2013002326A/es not_active Application Discontinuation
- 2011-09-01 RU RU2013115388/13A patent/RU2013115388A/ru not_active Application Discontinuation
- 2011-09-01 CN CN2011800536352A patent/CN103200828A/zh active Pending
- 2011-09-01 EP EP11752489.2A patent/EP2613645A1/en not_active Withdrawn
- 2011-09-01 WO PCT/EP2011/004421 patent/WO2012031720A1/en active Application Filing
Patent Citations (5)
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US4831129A (en) * | 1985-10-02 | 1989-05-16 | Roquette Freres | Directly compressible powdered maltitol and its process of preparation |
US5651829A (en) * | 1995-03-29 | 1997-07-29 | Roquette Freres | Maltitol composition and process for preparing it |
US20030099701A1 (en) * | 2001-05-10 | 2003-05-29 | Yamanouchi Pharmaceutical Co., Ltd. | Quick-disintegrating tablet in buccal cavity and manufacturing method thereof |
US20080020008A1 (en) * | 2005-01-24 | 2008-01-24 | Nikken Fine Chemical Co., Ltd. | Eutectic Crystalline Sugar Alcohol and Manufacturing Method Thereof |
US20110097401A1 (en) * | 2009-06-12 | 2011-04-28 | Meritage Pharma, Inc. | Methods for treating gastrointestinal disorders |
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20160209124A1 (en) * | 2013-08-29 | 2016-07-21 | Board Of Regents, The University Of Texas System | Thermal storage units, components thereof, and methods of making and using them |
WO2016001586A1 (fr) * | 2014-07-01 | 2016-01-07 | Roquette Freres | Nouvelle composition de produit de confiserie |
US10420354B2 (en) * | 2014-07-01 | 2019-09-24 | Roquette Freres | Composition of a confectionery product |
CN108697114A (zh) * | 2016-02-17 | 2018-10-23 | 罗盖特公司 | 增强的风味释放口香糖组合物 |
US20190246662A1 (en) * | 2016-02-17 | 2019-08-15 | Roquette Freres | Enhanced flavor release chewing gum composition |
CN115363127A (zh) * | 2016-02-17 | 2022-11-22 | 罗盖特公司 | 增强的风味释放口香糖组合物 |
CN108697114B (zh) * | 2016-02-17 | 2023-02-21 | 罗盖特公司 | 增强的风味释放口香糖组合物 |
US11666065B2 (en) * | 2016-02-17 | 2023-06-06 | Roquette Freres | Enhanced flavor release chewing gum composition |
Also Published As
Publication number | Publication date |
---|---|
BR112013005440A2 (pt) | 2016-05-17 |
EP2613645A1 (en) | 2013-07-17 |
KR20130138774A (ko) | 2013-12-19 |
CN103200828A (zh) | 2013-07-10 |
MX2013002326A (es) | 2013-03-18 |
WO2012031720A1 (en) | 2012-03-15 |
RU2013115388A (ru) | 2014-10-20 |
JP2013536694A (ja) | 2013-09-26 |
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